Mysegmenter Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mysegmenter Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MySegmenter (v2.0.0)
1
Total
1
Cleared
0
Denied
Mysegmenter Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dover, US.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mysegmenter Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mysegmenter Technologies, Inc.
1 devices